MAOA and mechanisms of panic disorder revisited: from bench to molecular psychotherapy

被引:79
作者
Reif, A. [1 ]
Richter, J. [2 ]
Straube, B. [3 ]
Hoefler, M. [4 ]
Lueken, U. [4 ]
Gloster, A. T. [4 ]
Weber, H. [1 ]
Domschke, K. [1 ,5 ]
Fehm, L. [6 ]
Stroehle, A. [7 ]
Jansen, A. [3 ]
Gerlach, A. [8 ]
Pyka, M. [3 ]
Reinhardt, I. [9 ]
Konrad, C. [3 ,5 ]
Wittmann, A. [7 ]
Pfleiderer, B. [10 ]
Alpers, G. W. [11 ,12 ]
Pauli, P. [13 ]
Lang, T. [14 ]
Arolt, V. [5 ]
Wittchen, H-U [4 ]
Hamm, A. [2 ]
Kircher, T. [3 ]
Deckert, J. [1 ]
机构
[1] Univ Wurzburg, Dept Psychiat Psychosomat & Psychotherapy, Psychiat Neurobiol & Bipolar Disorder Program, D-97080 Wurzburg, Germany
[2] Ernst Moritz Arndt Univ Greifswald, Dept Biol & Clin Psychol, Greifswald, Germany
[3] Univ Marburg, Dept Psychiat & Psychotherapy, Marburg, Germany
[4] Tech Univ Dresden, Inst Clin Psychol & Psychotherapy, Dept Psychol, D-01062 Dresden, Germany
[5] Univ Munster, Dept Psychiat & Psychotherapy, D-48149 Munster, Germany
[6] Humboldt Univ, Dept Psychol, D-10099 Berlin, Germany
[7] Charite, Dept Psychiat & Psychotherapy, D-13353 Berlin, Germany
[8] Univ Cologne, Inst Clin Psychol & Psychotherapy, D-50931 Cologne, Germany
[9] Rhein Westfal TH Aachen, Dept Psychiat & Psychotherapy, D-52062 Aachen, Germany
[10] Univ Munster, Dept Clin Radiol, D-48149 Munster, Germany
[11] Univ Mannheim, Sch Social Sci, Chair Clin & Biol Psychol, D-68131 Mannheim, Germany
[12] Univ Mannheim, Otto Selz Inst, D-68131 Mannheim, Germany
[13] Univ Wurzburg, Dept Psychol, D-97080 Wurzburg, Germany
[14] Inst Bremen, Bremen, Germany
关键词
behavioral avoidance task; fMRI; monoamine oxidase A; panic disorder; promoter polymorphism; therapygenetics; RANDOMIZED CONTROLLED-TRIAL; MONOAMINE-OXIDASE-A; FEAR EXTINCTION; GENE POLYMORPHISMS; NORRIE-DISEASE; HUMANS; AGORAPHOBIA; ANXIETY; PROMOTER; BEHAVIOR;
D O I
10.1038/mp.2012.172
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Panic disorder with agoraphobia (PD/AG) is a prevalent mental disorder featuring a substantial complex genetic component. At present, only a few established risk genes exist. Among these, the gene encoding monoamine oxidase A (MAOA) is noteworthy given that genetic variation has been demonstrated to influence gene expression and monoamine levels. Long alleles of the MAOA-uVNTR promoter polymorphism are associated with PD/AG and correspond with increased enzyme activity. Here, we have thus investigated the impact of MAOA-uVNTR on therapy response, behavioral avoidance and brain activity in fear conditioning in a large controlled and randomized multicenter study on cognitive behavioral therapy (CBT) in PD/AG. The study consisted of 369 PD/AG patients, and genetic information was available for 283 patients. Carriers of the risk allele had significantly worse outcome as measured by the Hamilton Anxiety scale (46% responders vs 67%, P = 0.017). This was accompanied by elevated heart rate and increased fear during an anxiety-provoking situation, that is, the behavioral avoidance task. All but one panic attack that happened during this task occurred in risk allele carriers and, furthermore, risk allele carriers did not habituate to the situation during repetitive exposure. Finally, functional neuroimaging during a classical fear conditioning paradigm evidenced that the protective allele is associated with increased activation of the anterior cingulate cortex upon presentation of the CS+ during acquisition of fear. Further differentiation between high-and low-risk subjects after treatment was observed in the inferior parietal lobes, suggesting differential brain activation patterns upon CBT. Taken together, we established that a genetic risk factor for PD/AG is associated with worse response to CBT and identify potential underlying neural mechanisms. These findings might govern how psychotherapy can include genetic information to tailor individualized treatment approaches.
引用
收藏
页码:122 / 128
页数:7
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